Works by Patiroglu, Turkan

Results: 103
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    Ãlkemizde kronik granülomatöz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi öncesi ve sonrası klinik verilerinin karşılaştırılması.

    Published in:
    2013
    By:
    • FİLİZ, Serkan;
    • Kocacik Uygun, Dilara Fatma;
    • Sanal, Özden;
    • CamcioĞLu, Yıldız;
    • Somer, Ayper;
    • Barlan, Işıl;
    • KiliÇ, Şebnem;
    • ReİSlİ, İsmail;
    • PatiroĞLu, Türkan;
    • Yildiran, Alişan;
    • ArtaÇ, Hasibe;
    • MetİN, Ayşe;
    • Aksu, Güzide;
    • Genel, Ferah;
    • ÖZtÜRk, Can;
    • ÇElmelİ, Fatih;
    • BİNgÖL, Ayşen;
    • YeĞİN, Olcay
    Publication type:
    Journal Article
    6

    lkemizde kronik granlomatz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi ncesi ve sonrası klinik verilerinin karşılaştırılması.

    Published in:
    Asthma Allergy Immunology / Astim Allerji Immunoloji, 2013, v. 11, n. 3, p. 153
    By:
    • FİLİZ, Serkan;
    • KOCACIK UYGUN, Dilara Fatma;
    • SANAL, Özden;
    • CAMCIOĞLU, Yıldız;
    • SOMER, Ayper;
    • BARLAN, Işıl;
    • KILIÇ, Şebnem;
    • REİSLİ, İsmail;
    • PATIROĞLU, Türkan;
    • YILDIRAN, Alişan;
    • ARTAÇ, Hasibe;
    • METİN, Ayşe;
    • AKSU, Güzide;
    • GENEL, Ferah;
    • ÖZTÜRK, Can;
    • ÇELMELİ, Fatih;
    • BİNGÖL, Ayşen;
    • YEĞİN, Olcay
    Publication type:
    Article
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    Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.

    Published in:
    2019
    By:
    • Yılmaz Karapınar, Deniz;
    • Patıroğlu, Türkan;
    • Metin, Ayşe;
    • Çalışkan, Ümran;
    • Celkan, Tiraje;
    • Yılmaz, Barış;
    • Karakaş, Zeynep;
    • Karapınar, Tuba H.;
    • Akıncı, Burcu;
    • Özkınay, Ferda;
    • Onay, Hüseyin;
    • Yeşilipek, Mehmet Akif;
    • Akar, Himmet Haluk;
    • Tüysüz, Gülen;
    • Tokgöz, Hüseyin;
    • Özdemir, Gül Nihal;
    • Aslan Kıykım, Ayça;
    • Karaman, Serap;
    • Kılınç, Yurdanur;
    • Oymak, Yeşim
    Publication type:
    journal article
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    Rare Coagulation Factor Deficiencies: Multicenter Experience With 188 Cases.

    Published in:
    Journal of the Child / Çocuk Dergisi, 2023, v. 23, n. 4, p. 349, doi. 10.26650/jchild.2023.1308877
    By:
    • Gök, Veysel;
    • Şahinoğlu, Esra Pekpak;
    • Tokgöz, Hüseyin;
    • Mutlu, Fatma Türkan;
    • Acıpayam, Can;
    • Karaman, Kamuran;
    • Tuncel, Defne Ay;
    • Ören, Ayşe Ceyda;
    • Şimşek, Ayşe;
    • Arslan, Bilal;
    • Ünal, Hatice Beyza;
    • Özcan, Alper;
    • Yılmaz, Ebru;
    • Akbayram, Sinan;
    • Karakükçü, Musa;
    • Öner, Ahmet Fayik;
    • Çalışkan, Ümran;
    • Patıroğlu, Türkan;
    • Ünal, Ekrem
    Publication type:
    Article
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    Neuroblastoma and Poland syndrome in a 15-year-old boy.

    Published in:
    Pediatrics International, 1997, v. 39, n. 6, p. 701, doi. 10.1111/j.1442-200X.1997.tb03672.x
    By:
    • ÇAKSEN, HÜSEYIN;
    • PATIROGLU, TÜRKAN;
    • ÖZDEMIR, M. AKIF;
    • PATIROGLU, TAHIR E.;
    • POYRAZOGLU, M. HAKAN;
    • TERCAN, MUSTAFA
    Publication type:
    Article
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    Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.

    Published in:
    Journal of Clinical Immunology, 2018, v. 38, n. 6, p. 699, doi. 10.1007/s10875-018-0533-8
    By:
    • Somekh, Ido;
    • Marquardt, Benjamin;
    • Liu, Yanshan;
    • Rohlfs, Meino;
    • Hollizeck, Sebastian;
    • Karakukcu, Musa;
    • Unal, Ekrem;
    • Yilmaz, Ebru;
    • Patiroglu, Turkan;
    • Cansever, Murat;
    • Frizinsky, Shirly;
    • Vishnvenska-Dai, Vicktoria;
    • Rechavi, Erez;
    • Stauber, Tali;
    • Simon, Amos J.;
    • Lev, Atar;
    • Klein, Christoph;
    • Kotlarz, Daniel;
    • Somech, Raz
    Publication type:
    Article
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    Multicentric analysis of childhood tuberculosis in Turkey.

    Published in:
    Turkish Journal of Pediatrics, 2013, v. 55, n. 2, p. 121
    By:
    • Aslan, Ayşe Tana;
    • Pekcan, Sevgi;
    • Kiper, Nural;
    • Uysal, Gülnar;
    • Gürkan, Fuat;
    • Patıroğlu, Türkan;
    • Öztürk, Mustafa;
    • Özen, Metehan;
    • Dağlı, Elif;
    • Doğru, Ülker;
    • Kocabaş, Emine;
    • Sarısoy, Özlem;
    • Koçak, Abdülkadir;
    • Uzuner, Nevin;
    • Reisli, İsmail;
    • Bolat, Ayşe;
    • Uğuz, Ayşen;
    • Karakelleoğlu, Cahit;
    • Uyan, Ayten;
    • Köse, Mehmet
    Publication type:
    Article
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    Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.

    Published in:
    Genome Medicine, 2015, v. 7, p. 1, doi. 10.1186/s13073-015-0244-1
    By:
    • Tesi, Bianca;
    • Lagerstedt-Robinson, Kristina;
    • Chiang, Samuel C. C.;
    • Bdira, Eya Ben;
    • Abboud, Miguel;
    • Belen, Burcu;
    • Devecioglu, Omer;
    • Fadoo, Zehra;
    • Yeoh, Allen E. J.;
    • Erichsen, Hans Christian;
    • Möttönen, Merja;
    • Haluk Akar, Himmet;
    • Hästbacka, Johanna;
    • Kaya, Zuhre;
    • Nunes, Susana;
    • Patiroglu, Turkan;
    • Sabel, Magnus;
    • Tugrul Saribeyoglu, Ebru;
    • Tvedt, Tor Henrik;
    • Unal, Ekrem
    Publication type:
    Article
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